Canonical Allele Identifier: CA394292119

Gene: TSC2

Linked Data

• ClinVar Variation Id: 1733712
• ClinVar RCV Id: RCV002452586
• COSMIC: COSM4736826 ; COSM4736827
• MyVariant Identifiers: chr16:g.2131649G>T (hg19) ; chr16:g.2081648G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2081648G>T , CM000678.2:g.2081648G>T	GRCh38
NC_000016.9:g.2131649G>T , CM000678.1:g.2131649G>T	GRCh37
NC_000016.8:g.2071650G>T	NCBI36
NG_005895.1:g.37343G>T , LRG_487:g.37343G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568566.6:c.*2082G>T	ENSP00000455997.2:n.*2082G>T
ENST00000642206.2:c.3580G>T	ENSP00000495146.2:p.Asp1194Tyr
ENST00000642365.2:c.3661G>T	ENSP00000495459.2:p.Asp1221Tyr
ENST00000644417.2:c.*4113G>T	ENSP00000493912.2:n.*4113G>T
ENST00000646464.2:c.*4586G>T	ENSP00000496610.2:n.*4586G>T
ENST00000219476.9:c.3664G>T MANE Select	ENSP00000219476.3:p.Asp1222Tyr
ENST00000350773.9:c.3664G>T	ENSP00000344383.4:p.Asp1222Tyr
ENST00000401874.7:c.3532G>T	ENSP00000384468.2:p.Asp1178Tyr
ENST00000568454.6:c.3565G>T	ENSP00000454487.1:p.Asp1189Tyr
ENST00000642365.1:c.2318G>T
ENST00000642561.1:c.3535G>T	ENSP00000495099.1:p.Asp1179Tyr
ENST00000642797.1:c.3535G>T	ENSP00000493846.1:p.Asp1179Tyr
ENST00000642936.1:c.3532G>T	ENSP00000494514.1:p.Asp1178Tyr
ENST00000643088.1:c.3532G>T	ENSP00000494747.1:p.Asp1178Tyr
ENST00000643426.1:n.1312G>T
ENST00000643533.1:n.174G>T
ENST00000643946.1:c.3664G>T	ENSP00000495927.1:p.Asp1222Tyr
ENST00000644043.1:c.3535G>T	ENSP00000496262.1:p.Asp1179Tyr
ENST00000644329.1:c.3532G>T	ENSP00000496611.1:p.Asp1178Tyr
ENST00000644335.1:c.3535G>T	ENSP00000496317.1:p.Asp1179Tyr
ENST00000644399.1:c.3654G>T
ENST00000644722.1:n.810G>T
ENST00000645024.1:n.1817G>T
ENST00000646388.1:c.3664G>T	ENSP00000495921.1:p.Asp1222Tyr
ENST00000646634.1:n.2548G>T
ENST00000646674.1:n.279G>T
ENST00000647042.1:n.956G>T
ENST00000647180.1:n.144G>T
ENST00000219476.7:c.3664G>T	ENSP00000219476.3:p.Asp1222Tyr
ENST00000350773.8:c.3664G>T	ENSP00000344383.4:p.Asp1222Tyr
ENST00000382538.10:c.3388G>T	ENSP00000371978.6:p.Asp1130Tyr
ENST00000401874.6:c.3532G>T	ENSP00000384468.2:p.Asp1178Tyr
ENST00000439117.6:c.*2831G>T	ENSP00000406980.2:n.*2831G>T
ENST00000439673.6:c.3424G>T	ENSP00000399232.2:p.Asp1142Tyr
ENST00000497886.5:n.1491G>T
ENST00000568454.5:c.3565G>T	ENSP00000454487.1:p.Asp1189Tyr
NM_000548.3:c.3664G>T , LRG_487t1:c.3664G>T	NP_000539.2:p.Asp1222Tyr
NM_001077183.1:c.3532G>T	NP_001070651.1:p.Asp1178Tyr
NM_001114382.1:c.3664G>T	NP_001107854.1:p.Asp1222Tyr
XM_005255529.3:c.3535G>T	XP_005255586.2:p.Asp1179Tyr
XM_005255531.3:c.3535G>T	XP_005255588.2:p.Asp1179Tyr
XM_011522636.1:c.3664G>T	XP_011520938.1:p.Asp1222Tyr
XM_011522637.1:c.3661G>T	XP_011520939.1:p.Asp1221Tyr
XM_011522638.1:c.3553G>T	XP_011520940.1:p.Asp1185Tyr
XM_011522639.1:c.3535G>T	XP_011520941.1:p.Asp1179Tyr
XM_011522640.1:c.3532G>T	XP_011520942.1:p.Asp1178Tyr
XM_011522641.1:c.3424G>T	XP_011520943.1:p.Asp1142Tyr
NM_000548.4:c.3664G>T	NP_000539.2:p.Asp1222Tyr
NM_001077183.2:c.3532G>T	NP_001070651.1:p.Asp1178Tyr
NM_001114382.2:c.3664G>T	NP_001107854.1:p.Asp1222Tyr
NM_001318827.1:c.3424G>T	NP_001305756.1:p.Asp1142Tyr
NM_001318829.1:c.3388G>T	NP_001305758.1:p.Asp1130Tyr
NM_001318831.1:c.2932G>T	NP_001305760.1:p.Asp978Tyr
NM_001318832.1:c.3565G>T	NP_001305761.1:p.Asp1189Tyr
NM_001363528.1:c.3535G>T	NP_001350457.1:p.Asp1179Tyr
NM_021055.2:c.3535G>T	NP_066399.2:p.Asp1179Tyr
XM_005255531.4:c.3535G>T	XP_005255588.2:p.Asp1179Tyr
XM_011522636.2:c.3664G>T	XP_011520938.1:p.Asp1222Tyr
XM_011522637.2:c.3661G>T	XP_011520939.1:p.Asp1221Tyr
XM_011522638.2:c.3826G>T	XP_011520940.2:p.Asp1276Tyr
XM_011522639.2:c.3535G>T	XP_011520941.1:p.Asp1179Tyr
XM_011522640.2:c.3532G>T	XP_011520942.1:p.Asp1178Tyr
XM_017023615.1:c.3661G>T	XP_016879104.1:p.Asp1221Tyr
XM_017023616.1:c.3532G>T	XP_016879105.1:p.Asp1178Tyr
XM_017023617.1:c.3697G>T	XP_016879106.1:p.Asp1233Tyr
XM_017023618.1:c.2320G>T	XP_016879107.1:p.Asp774Tyr
XM_024450413.1:c.3532G>T	XP_024306181.1:p.Asp1178Tyr
NM_000548.5:c.3664G>T MANE Select	NP_000539.2:p.Asp1222Tyr
NM_001370404.1:c.3532G>T	NP_001357333.1:p.Asp1178Tyr
NM_001370405.1:c.3535G>T	NP_001357334.1:p.Asp1179Tyr
NM_001077183.3:c.3532G>T	NP_001070651.1:p.Asp1178Tyr
NM_001114382.3:c.3664G>T	NP_001107854.1:p.Asp1222Tyr
NM_001318827.2:c.3424G>T	NP_001305756.1:p.Asp1142Tyr
NM_001318829.2:c.3388G>T	NP_001305758.1:p.Asp1130Tyr
NM_001318831.2:c.2932G>T	NP_001305760.1:p.Asp978Tyr
NM_001318832.2:c.3565G>T	NP_001305761.1:p.Asp1189Tyr
NM_001363528.2:c.3535G>T	NP_001350457.1:p.Asp1179Tyr
NM_021055.3:c.3535G>T	NP_066399.2:p.Asp1179Tyr